Monthly Archives: July 2014

Emma’s Story – Video

Posted: July 25, 2014 at 8:40 am


Emma #39;s Story
Jeanette and David Nucifora have three daughters. There were all born at Credit Valley Hospital in Mississauga. At birth, they chose to save the cord blood stem cells for all three girls. This...

By: Cells for Life

See original here:
Emma's Story - Video

Posted in Stem Cell Videos | Comments Off on Emma’s Story – Video

STEM CELL THERAPY SUPERNOVA – Video

Posted: July 25, 2014 at 8:40 am


STEM CELL THERAPY SUPERNOVA
We implant EMBRYONIC STEM CELLS from our STEM CELL BANK This is state-of-the-art ADVANTAGE for it eliminates the suffering and pain from liposuction(fat remo...

By: Leong Lau

Continued here:
STEM CELL THERAPY SUPERNOVA - Video

Posted in Stem Cell Treatments | Comments Off on STEM CELL THERAPY SUPERNOVA – Video

"Stem Cells Dr. Nathan Newman" – Sean Wroe Jeuness Global Distributor – Video

Posted: July 25, 2014 at 4:53 am


"Stem Cells Dr. Nathan Newman" - Sean Wroe Jeuness Global Distributor
Stem Cells are the future of health and beauty. Jeunesse Global is at the forefront of this incredible Stem Cell Technology. Sean Wroe is a Jeunesse Global Distributor leading the way. http://www.seanwroe...

By: Sean Wroe

See the original post here:
"Stem Cells Dr. Nathan Newman" - Sean Wroe Jeuness Global Distributor - Video

Posted in Stem Cells | Comments Off on "Stem Cells Dr. Nathan Newman" – Sean Wroe Jeuness Global Distributor – Video

Emma's Story – Video

Posted: July 25, 2014 at 4:53 am


Emma #39;s Story
Jeanette and David Nucifora have three daughters. There were all born at Credit Valley Hospital in Mississauga. At birth, they chose to save the cord blood stem cells for all three girls. This...

By: Cells for Life

Go here to read the rest:
Emma's Story - Video

Posted in Stem Cells | Comments Off on Emma's Story – Video

Stem Cells: Promises and Reality

Posted: July 25, 2014 at 4:53 am

Renowned Israeli stem-cell researcher in Fairfield Aug. 6

By Cindy Mindell

Dr. Yaqub Hanna

A leading Israeli scientist who has pioneered groundbreaking stem-cell reprogamming research will discuss his work on Wednesday, Aug. 6 at Jewish Senior Services in Fairfield.

Together with a team of researchers at the Weizmann Institute of Science Department of Molecular Genetics in Rehovot, Israel, Dr. Jacob (Yaqub) Hanna has overcome a major roadblock in the use of human stem cells for medical purposes. Funded by a grant from the Israel Cancer Research Fund, their pioneering breakthrough was recently published in the peer-reviewed international science journal, Nature.

Its not only Hannas work that is note-worthy: the award-winning research scientist is a Palestinian living in Israel, a native of Kafr Rama in the Galilee and the son of two medical doctors.

Hanna earned a BS in medical sciences summa cum laude in 2001, an MS in microbiology and immunology in 2003, and a PhD-MD in immunology summa cum laude in 2007, all from the Hebrew University of Jerusalem, where he was among the top five percent of all Israeli medical-school graduates. After completing his PhD, Hanna decided to abandon clinical medicine and focus on research, and spent four years conducting postdoctoral research in the lab, part of the Whitehead Institute for Biomedical Research at MIT.

During his postdoctoral work, Hanna was the first non-American to receive a prestigious Novartis Fellowship from the Helen Hay Whitney Foundation. He joined the Weizmann Institute Department of Molecular Genetics upon his return to Israel in 2011. That year, he received the Clore Prize for distinguished new faculty at the Weizmann Institute and was accepted as a Yigal Alon Program Scholar for junior faculty in Israel. He is also the recipient of the Wolf Foundations Krill Prize for Excellence in Scientific Research and the 2013 Rappaport Prize in Biomedical Research.

Hanna has had to find a way to navigate between his personal and professional identities.

Read more:
Stem Cells: Promises and Reality

Posted in Stem Cells | Comments Off on Stem Cells: Promises and Reality

New knee op using stem cells could stop arthritis and extend sporting careers

Posted: July 25, 2014 at 4:52 am

Surgeons at the University Hospital Southampton have designed the new procedure to coat damaged cartilage with stem cells taken from the hip If successful, it will regenerate the remaining tissue, creating a permanent 'like-for-like' replacement for the first time Cartilage is a tough tissue covering the surface of joints and enables bones to slide over one another, reducing friction and acting as a shock absorber

By Lizzie Parry

Published: 07:05 EST, 23 July 2014 | Updated: 07:21 EST, 23 July 2014

221 shares

11

View comments

Surgeons have designed a new operation which they hope could prevent the development of arthritis and extend sporting careers.

The procedure, which is currently being trialled at Southampton General Hospital, involves coating damaged cartilage with stem cells, taken from a patients own hip, and surgical glue.

If successful, it will regenerate the remaining tissue and create a permanent 'like-for-like' replacement for the first time.

Surgeons at University Hospital Southampton have pioneered a new operation to treat knee injuries, which they hope will extend sporting careers. Argentinian striker Luis Suarez had an operation to remove his damaged meniscus, part of the cartilage in the knee, prior to the World Cup

Read the original post:
New knee op using stem cells could stop arthritis and extend sporting careers

Posted in Stem Cells | Comments Off on New knee op using stem cells could stop arthritis and extend sporting careers

Joslin Scientists Create the First IPS Cells to Offer Human Model of Insulin Resistance

Posted: July 25, 2014 at 4:52 am

Contact Information

Available for logged-in reporters only

Newswise BOSTON July 24, 2014 Japanese biologist Shinya Yamanaka won a Nobel Prize in 2012 for discovering how to create induced pluripotent stem cells (iPSCs), cells derived from normal adult cells that have the ability to differentiate into almost any other kind of cells. Scientists at Joslin Diabetes Center now have created the first iPSCs that offer a human model of insulin resistance, a key driver of type 2 diabetes.

This is one of the very first studies of human iPSC models for type 2 diabetes, and it points out the power of this technology to look at the nature of diabetes, which is complex and may be different in different individuals, says C. Ronald Kahn, MD, Joslins Chief Academic Officer and the Mary K. Iacocca Professor of Medicine at Harvard Medical School.

Until now, scientists examining the causes and effects of insulin resistance have struggled with a general lack of human cell lines from tissues such as muscle, fat and liver that respond significantly to insulin, Kahn says. Studying insulin resistance as it progresses through pre-clinical stages of type 2 diabetes has been particularly challenging.

There have been no good human cell models to study insulin resistance, but such cells can now be made with iPSCs, says Kahn, co-senior author on a paper about the study published in the journal Diabetes.

Generation of iPSCs typically starts with fibroblasts (connective tissue cells) from skin samples. Kahn and his colleagues used fibroblasts from three patients with severe insulin resistance brought on by mutations in the gene for the insulin receptor (IR)a molecule that crosses the cell membrane and plays a key role in insulin signaling and glucose metabolism.

The Joslin researchers reprogrammed the fibroblasts into iPSCs by using viral procedures that activated four genes that together maintain cells in the iPSC state. The scientists then looked at gene activation in insulin signaling pathways for iPSCs and fibroblasts with IR mutations, and for corresponding cells derived from people without those mutations.

Among the study findings, IR mutations alter expression of many genes both in fibroblasts and iPSCs compared to normal cells, but the impact is very much dependent on the cell type, says Kahn. You see one type of expression pattern in the fibroblasts and a different type of pattern in the iPSCs.

Insulin is a key ingredient for the growth and proliferation of normal stem cells, and the study demonstrated that insulin resistance also reduces the ability of the iPSCs to grow and proliferate. That defect may represent a previously unrecognized mechanism that aids in developing diabetes, Kahn says, as well as helping to explain the problems in wound healing, tissue repair and even beta-cell growth that are common among people with diabetes.

View post:
Joslin Scientists Create the First IPS Cells to Offer Human Model of Insulin Resistance

Posted in Stem Cells | Comments Off on Joslin Scientists Create the First IPS Cells to Offer Human Model of Insulin Resistance

Tissue Collection Aids Search for Neurologic and Neuromuscular Disease Causes and Cures

Posted: July 25, 2014 at 4:50 am

Contact Information

Available for logged-in reporters only

Newswise LOS ANGELES (July 24, 2014) Like other major research centers studying genetic causes of uncommon and poorly understood nervous system disorders, Cedars-Sinai maintains a growing collection of DNA and tissue samples donated by patients.

What sets Cedars-Sinais Repository of Neurologic and Neuromuscular Disorders apart is its special emphasis on tissue collection part of its focus on creating future individualized treatments for patients.

One of our major priorities is to advance the concept of personalized medicine. The idea is to take DNA from a patient, look at the cells derived from their tissue, and try to understand why this particular person got this disease. Then we can determine which therapy or therapies would work for each individual by first testing their cells. Many centers look at the genetics; ours is dedicated to looking at the genetics and the patients tissues, combining the two to understand how to treat the disease, said Robert H. Baloh, MD, PhD, director of neuromuscular medicine in the Department of Neurology and director of the ALS Program for research and treatment of amyotrophic lateral sclerosis, or Lou Gehrigs disease.

This individualized treatment approach depends on collaborative efforts among doctors and researchers who treat and study individual diseases and scientists at the Cedars-Sinai Regenerative Medicine Institute, one of a very few hospital-based centers devoted to stem cell research. The teams work together to discover disease-generating molecular and cellular defects, make disease-in-a-dish models and begin to fashion personalized stem cell-based research interventions.

We know that nearly every disease has some genetic component some more than others so we collect DNA for research to identify those genetic elements. But weve also expanded our focus to include the collection of skin and blood samples that can be turned into specialized stem cells. Patients are usually very willing to donate tissue to try and help us understand the causes of their neurologic or neuromuscular disease, said Baloh, a member of the Brain Program at the Regenerative Medicine Institute.

Baloh and colleagues recently showed this approach is feasible, using skin biopsies from patients with ALS. With induced pluripotent stem cells, or iPSCs, they created ALS neurons in a lab dish. Then, inserting molecules made of small stretches of genetic material, they blocked the damaging effects of a defective gene. This provided proof of concept for a new therapeutic strategy an important step in moving research findings into clinical trials.

Baloh, the repositorys principal investigator, has a particular interest in ALS and other neuromuscular disorders, but DNA, tissue and data collection is conducted for Cedars-Sinai neuroscience researchers studying virtually any disease. And its holdings can have widespread influence: Repositories of genetic material enable scientists studying similar diseases at multiple research centers to access patient data in larger quantities than any single site could provide.

We work with many other research institutions across the country to share the samples themselves as well as de-identified information about the patients what disease they have, the severity of their disease, and similar disorder-related details. This improves our ability to find new gene abnormalities, because it cant always be done with just tens or even hundreds of patients. We may need thousands of patients, especially for very rare genetic forms of disease that have very subtle genetic effects. Therefore, we study our own patients in great detail, but we also share our resources more broadly, said Baloh, adding that genetic discoveries often have implications even for patients who dont have genetic forms of disease.

Go here to read the rest:
Tissue Collection Aids Search for Neurologic and Neuromuscular Disease Causes and Cures

Posted in Genetic medicine | Comments Off on Tissue Collection Aids Search for Neurologic and Neuromuscular Disease Causes and Cures

Experiments prove 'stemness' of individual immune memory cells

Posted: July 25, 2014 at 4:47 am

PUBLIC RELEASE DATE:

24-Jul-2014

Contact: Vera Siegler vera.siegler@tum.de 49-892-892-2731 Technische Universitaet Muenchen

This news release is available in German.

The immune system has evolved to recognize and respond to threats to health, and to provide life-long memory that prevents recurrent disease. A detailed understanding of the mechanism underlying immunologic memory, however, has remained elusive. Since 2001, various lines of research have converged to support the hypothesis that the persistence of immune memory arises from a reservoir of immune cells with stem-cell-like potential. Until now, there was no conclusive evidence, largely because experiments could only be carried out on populations of cells. This first strict test of the stem cell hypothesis of immune memory was based on mapping the fates of individual T cells and their descendants over several generations.

That experimental capability was developed through a long-term collaboration, focused on clinical cell processing and purification, between researchers based in Munich and Seattle. Since 2009, the groups of Prof. Dirk Busch at the Technische Universitt Mnchen (TUM) and Prof. Stanley Riddell at the Fred Hutchinson Cancer Research Center have combined their technological and clinical expertise under the auspices of the TUM Institute for Advanced Study. The University of Heidelberg, the University of Dsseldorf, the Helmholtz Center Munich, the German Cancer Research Center (DKFZ), and the National Center for Infection Research (DZIF) also contributed to the present study.

Homing In On The "Stemness" of T Cells

After generating an immune response in laboratory animals, TUM researchers Patricia Graef and Veit Buchholz separated complex "killer" T cell populations enlisted to fight the immediate or recurring infection. Within these cell populations, they then identified subgroups and proceeded with a series of single-cell adoptive transfer experiments, in which the aftermath of immune responses could be analyzed in detail. Here the ability to identify and characterize the descendants of individual T cells through several generations was crucial.

The researchers first established that a high potential for expansion and differentiation in a defined subpopulation, called "central memory T cells," does not depend exclusively on any special source such as bone marrow, lymph nodes, or spleen. This supported but did not yet prove the idea that certain central memory T cells are, effectively, adult stem cells. Further experiments, using and comparing both memory T cells and so-called naive T cells that is, mature immune cells that have not yet encountered their antigen enabled the scientists to home in on stem-cell-like characteristics and eliminate other possible explanations.

Step by step, the results strengthened the case that the persistence of immune memory depends on the "stemness" of the subpopulation of T cells termed central memory T cells: Individual central memory T cells proved to be "multipotent," meaning that they can generate diverse types of offspring to fight an infection and to remember the antagonist. Further, these individual T cells self-renew into secondary memory T cells that are, again, multipotent at the single-cell level. And finally, individual descendants of secondary memory T cells are capable of fully restoring the capacity for a normal immune response.

View original post here:
Experiments prove 'stemness' of individual immune memory cells

Posted in Cell Therapy | Comments Off on Experiments prove 'stemness' of individual immune memory cells

Stem cell agency tightens ethics rules

Posted: July 25, 2014 at 4:45 am

Stem cell agency President C. Randal Mills (left) and Chairman of the Board Jonathan Thomas.

Responding to his predecessor's ethically controversial departure, the president and chief executive of California's stem cell agency said Thursday he is taking legal steps to minimize conflicts of interests with those who have business before the agency.

C. Randal Mills said he will not take a job with any company funded by the California Institute for Regenerative Medicine for one year after he departs the agency. In addition, he also will not accept gifts or travel payments from any company, institution or person who gets agency funding.

Mills' action, announced at the agency's meeting in Millbrae, will be enforced with a legal agreement he will sign. His action comes less than a month after he replaced Alan Trounson as the agency chief. One week after his departure, CIRM-funded StemCells Inc. announced it had appointed Trounson to its board. StemCells Inc. had received an award of nearly $20 million from the agency to develop a therapy for Alzheimers disease.

While Trounson's appointment wasn't illegal, critics said it was unseemly for him to join a company that had received agency funding so soon after he left CIRM. An ethical controversy could harm the agency's chances of getting more funding from California voters, who gave the agency $3 billion with the passage of Proposition 71 in 2004.

Mills said the new rules apply only to himself, because of his central role at CIRM.

"This specifically addresses an issue where an individual in an organization has a disproportionate amount of power, and I want to make sure it's known that power will not be abused," Mills said.

Mills made the right decision, said Jeanne Loring, a CIRM-funded stem cell researcher at The Scripps Research Institute.

"There's a difference between what is legal and what is ethical," said Loring, who attended the meeting. "And he's going to be pushing the needle a lot more toward the ethical side without worrying whether he can get away with stuff."

John Simpson of Santa Monica-based Consumer Watchdog, who has often criticized CIRM for conflicts of interest, also praised the decision.

See the article here:
Stem cell agency tightens ethics rules

Posted in Stem Cell Therapy | Comments Off on Stem cell agency tightens ethics rules